1-(Trifluoroacetyl)imidazole
For GC derivatization, ≥98.5%
- Product Code: 93714
Alias:
N-trifluoroacetylimidazole
CAS:
1546-79-8
| Molecular Weight: | 164.09 g./mol | Molecular Formula: | C₅H₃F₃N₂O |
|---|---|---|---|
| EC Number: | 216-282-5 | MDL Number: | MFCD00014501 |
| Melting Point: | Boiling Point: | 137 °C(lit.) | |
| Density: | 1.442 g/mL at 25 °C(lit.) | Storage Condition: | 2~8°C |
Product Description:
1-(Trifluoroacetyl)imidazole is widely used in organic synthesis as a versatile reagent. It is particularly effective in the acylation of alcohols, amines, and thiols, enabling the introduction of the trifluoroacetyl group into various molecules. This compound is also employed in the preparation of trifluoroacetyl-protected intermediates, which are crucial in peptide synthesis and the development of pharmaceuticals. Additionally, it serves as a catalyst or activator in certain chemical reactions, enhancing reaction efficiency and selectivity. Its applications extend to the modification of biomolecules, aiding in the study of biochemical processes and the design of novel therapeutic agents.
Product Specification:
| Test | Specification |
|---|---|
| COLOR TEST | 0-300 |
| PurityGC | 98.5 100% |
| APPEARANCE | Colorless to light yellow liquid |
| INFRARED SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | ฿9,234.00 |
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| 10.000 | 10-20 days | ฿17,559.00 |
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1-(Trifluoroacetyl)imidazole
1-(Trifluoroacetyl)imidazole is widely used in organic synthesis as a versatile reagent. It is particularly effective in the acylation of alcohols, amines, and thiols, enabling the introduction of the trifluoroacetyl group into various molecules. This compound is also employed in the preparation of trifluoroacetyl-protected intermediates, which are crucial in peptide synthesis and the development of pharmaceuticals. Additionally, it serves as a catalyst or activator in certain chemical reactions, enhancing reaction efficiency and selectivity. Its applications extend to the modification of biomolecules, aiding in the study of biochemical processes and the design of novel therapeutic agents.
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